PřF:C7415 Structure and Reactivity - Course Information
C7415 Structure and Reactivity
Faculty of ScienceAutumn 2013
- Extent and Intensity
- 0/1/0. 1 credit(s) (fasci plus compl plus > 4). Type of Completion: z (credit).
- Teacher(s)
- prof. RNDr. Petr Klán, Ph.D. (lecturer)
- Guaranteed by
- prof. RNDr. Petr Klán, Ph.D.
Department of Chemistry – Chemistry Section – Faculty of Science
Contact Person: prof. RNDr. Petr Klán, Ph.D.
Supplier department: Department of Chemistry – Chemistry Section – Faculty of Science - Timetable
- Thu 11:00–11:50 A08/309
- Prerequisites
- NOW( C7410 Structure and Reactivity )
organic chemistry, physical chemistry, physics - Course Enrolment Limitations
- The course is also offered to the students of the fields other than those the course is directly associated with.
- fields of study / plans the course is directly associated with
- Analytical Chemistry (Eng.) (programme PřF, D-CH4)
- Analytical Chemistry (programme PřF, D-CH) (2)
- Analytical Chemistry (programme PřF, D-CH4)
- Inorganic Chemistry (Eng.) (programme PřF, D-CH4)
- Inorganic Chemistry (programme PřF, D-CH) (2)
- Physical Chemistry (programme PřF, D-CH) (2)
- Macromolecular Chemistry (programme PřF, D-CH) (2)
- Environmental Chemistry (programme PřF, D-CH) (2)
- Organic Chemistry (programme PřF, D-CH) (2)
- Organic Chemistry (programme PřF, M-CH)
- Organic Chemistry (programme PřF, N-CH)
- Course objectives
- Seminar. At the end of the course students should be able to understand and practise what was discussed in the course of Structure and Reactivity (C7410).
- Syllabus
- 1. Structure and reactivity relationship. Calibration points in chemistry. Inner parameters of the structure and its deformations. Physical properties caused by (a) geometry of nuclei, (b) electron density and its change. Activation and driving force of the chemical reactions. 2. Stability of molecules. Thermodynamic additive calculations. Conformations of acyclic and cyclic hydrocarbons. Heteroatom effects. Hyperconjugation. Anomeric effect. 3. Aromaticity a antiaromaticity. Aromatic ions and dipoles. Aromaticity of the transition state in the pericyclic reactions. 4. Non-covalent interactions and solvent effects. Solutions. Hughes-Ingold principles. H-bonding. Hydrophobic effect. Molecular recognition. 5. Proton transfer. Acid-base equilibria. 6. Chemical kinetics and reactivity. HSAB. Nucleophiles and electrophiles. Rate constants. Hammond and Curtin-Hammond principles. Driving force of the reactions. 7. Thermodynamics and kinetics - the tools to study chemical reactions. LFER. Hammett equation. Taft equation. QSAR. Kinetic isotope effects. Entropy vs. enthalpy. 8. Catalysis. Transition metal catalysis. Heterogeneous catalysis. Enzymatic catalysis. Brönsted catalysis. 9. Electron transfer. Marcus equation. 10. Photochemistry and photophysics. 11. Spin chemistry. Magnetic field effects. 12. Non-classical activation of chemical reactions.
- Literature
- recommended literature
- E. V. Anslyn, D. A. Dougherty: Modern Physical Organic Chemistry. University Science Books, Kausalito, California 2005. ISBN 1-891389-9.
- Teaching methods
- Seminar - a calss discussion
- Assessment methods
- Attendance and working out of class assignment.
- Language of instruction
- Czech
- Follow-Up Courses
- Further Comments
- The course can also be completed outside the examination period.
The course is taught annually. - Listed among pre-requisites of other courses
- Enrolment Statistics (Autumn 2013, recent)
- Permalink: https://is.muni.cz/course/sci/autumn2013/C7415